Variant report

Variant	esv1826871
Chromosome Location	chr4:69363077-69527406
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:872)
CpG islands
(count:428)
Chromatin interactive
region (count:6)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:872 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
8	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
9	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
10	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
11	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
12	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
13	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
19	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
20	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
25	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
26	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
27	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
28	CTCF	chr4:69523122-69523163	K562	blood:	n/a	n/a
29	CTCF	chr4:69434848-69435081	A549	lung:	n/a	n/a
30	CTCF	chr4:69434820-69434970	GM12873	blood:	n/a	n/a
31	CTCF	chr4:69364108-69364453	H1-hESC	embryonic stem cell:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
32	CTCF	chr4:69523109-69523218	Gliobla	brain:	n/a	n/a
33	CTCF	chr4:69364238-69364417	GM19239	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
34	CTCF	chr4:69443417-69443543	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr4:69523051-69523262	GM19240	blood:	n/a	n/a
36	CTCF	chr4:69434910-69435031	GM10266	blood:	n/a	n/a
37	CTCF	chr4:69443420-69443570	GM12875	blood:	n/a	n/a
38	CTCF	chr4:69443440-69443590	GM12869	blood:	n/a	n/a
39	CTCF	chr4:69384740-69384847	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr4:69434820-69434970	SAEC	small airway:	n/a	n/a
41	CTCF	chr4:69443440-69443590	GM12874	blood:	n/a	n/a
42	CTCF	chr4:69364280-69364430	NHDF-neo	bronchial:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
43	CTCF	chr4:69364240-69364390	HA-sp	spinal cord:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
44	CTCF	chr4:69364160-69364310	HAc	cerebellar:	n/a	n/a
45	CTCF	chr4:69443400-69443550	GM12873	blood:	n/a	n/a
46	CTCF	chr4:69364240-69364390	GM12869	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
47	CTCF	chr4:69364180-69364330	NHEK	skin:	n/a	chr4:69364310-69364328 chr4:69364311-69364327
48	CTCF	chr4:69443120-69443270	GM12866	blood:	n/a	n/a
49	CTCF	chr4:69419814-69419975	GM10248	blood:	n/a	n/a
50	CTCF	chr4:69419821-69419967	HepG2	liver:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69514031-69514081	HCF	heart:	n/a
2	chr4:69514031-69514081	HCF	heart:	n/a
3	chr4:69381368-69381418	GM12891	blood:	n/a
4	chr4:69435250-69435300	HUVEC	blood vessel:	n/a
5	chr4:69435593-69435643	T-47D	breast:	n/a
6	chr4:69434475-69434525	AoSMC	blood vessel:	n/a
7	chr4:69522639-69522689	GM12878	blood:	n/a
8	chr4:69522639-69522689	PANC-1	pancreas:	n/a
9	chr4:69435250-69435300	T-47D	breast:	n/a
10	chr4:69435593-69435643	GM12892	blood:	n/a
11	chr4:69435593-69435643	A549	lung:	n/a
12	chr4:69381368-69381418	GM06990	blood:	n/a
13	chr4:69435601-69435651	HCT-116	colon:	n/a
14	chr4:69435593-69435643	NB4	blood:	n/a
15	chr4:69435250-69435300	RPTEC	kidney:	n/a
16	chr4:69381368-69381418	NB4	blood:	n/a
17	chr4:69522639-69522689	HepG2	liver:	n/a
18	chr4:69435601-69435651	Caco-2	colon:	n/a
19	chr4:69522639-69522689	HCF	heart:	n/a
20	chr4:69435593-69435643	PFSK-1	brain:	n/a
21	chr4:69381368-69381418	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:69522639-69522689	GM12891	blood:	n/a
23	chr4:69381368-69381418	PFSK-1	brain:	n/a
24	chr4:69435250-69435300	AG04450	lung:	fetal
25	chr4:69435601-69435651	Jurkat	blood:	n/a
26	chr4:69435250-69435300	SK-N-SH_RA	brain:	n/a
27	chr4:69381368-69381418	SKMC	muscle:	n/a
28	chr4:69381368-69381418	LNCaP	prostate:	n/a
29	chr4:69381368-69381418	HRCEpiC	kidney:	n/a
30	chr4:69522639-69522689	HRCEpiC	kidney:	n/a
31	chr4:69434475-69434525	Caco-2	colon:	n/a
32	chr4:69514031-69514081	HEK293	kidney:	embryo
33	chr4:69435250-69435300	GM12891	blood:	n/a
34	chr4:69435250-69435300	HepG2	liver:	n/a
35	chr4:69522639-69522689	AG10803	skin:	n/a
36	chr4:69522639-69522689	AG09319	gingival:	n/a
37	chr4:69522639-69522689	H1-hESC	embryonic stem cell:	embryo
38	chr4:69435601-69435651	AG09319	gingival:	n/a
39	chr4:69514031-69514081	Hepatocyte	liver:	n/a
40	chr4:69435601-69435651	HRPEpiC	eye:	n/a
41	chr4:69434475-69434525	GM19239	blood:	n/a
42	chr4:69522639-69522689	SK-N-SH	brain:	n/a
43	chr4:69434475-69434525	HCT-116	colon:	n/a
44	chr4:69381368-69381418	GM12892	blood:	n/a
45	chr4:69435601-69435651	HRE	kidney:	n/a
46	chr4:69381368-69381418	AG09319	gingival:	n/a
47	chr4:69522639-69522689	NB4	blood:	n/a
48	chr4:69522639-69522689	NT2-D1	testis:	n/a
49	chr4:69435601-69435651	GM12878	blood:	n/a
50	chr4:69522639-69522689	GM19239	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
2	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
3	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
4	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
5	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
6	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737
2	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736
3	lnc-UGT2B17-1	chr4:69382627-69383365	NONHSAT096733
4	lnc-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733
5	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
6	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737

No data

Variant related genes	Relation type
ENSG00000249472	TF binding region
ENSG00000251074	TF binding region
ENSG00000251101	TF binding region
UGT2B17	TF binding region
UGT2B29P	TF binding region
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B29P	CpG island
ENSG00000083896	chromatin interactions
ENSG00000249985	chromatin interactions
ENSG00000272626	chromatin interactions

Extended variants
information (count: 4417 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4417 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78295079	chr4:69363077-69363078	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs34436963	chr4:69363119-69363120	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs191092556	chr4:69363131-69363132	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs531153394	chr4:69363164-69363165	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs535157634	chr4:69363253-69363254	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs555450876	chr4:69363265-69363266	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs574902747	chr4:69363267-69363268	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs537675786	chr4:69363294-69363295	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs183686726	chr4:69363300-69363301	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs577593669	chr4:69363310-69363311	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs546558270	chr4:69363335-69363336	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs559778800	chr4:69363336-69363337	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs199642691	chr4:69363399-69363400	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs573191336	chr4:69363403-69363404	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs144902755	chr4:69363407-69363408	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs386675586	chr4:69363421-69363422	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs142222888	chr4:69363422-69363423	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs199822457	chr4:69363428-69363429	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs549339672	chr4:69363429-69363430	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs563980022	chr4:69363436-69363437	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs2603155	chr4:69363473-69363474	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs546494386	chr4:69363493-69363494	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs573644443	chr4:69363517-69363518	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs2603154	chr4:69363530-69363531	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs535448947	chr4:69363573-69363574	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs188401824	chr4:69363587-69363588	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs2708672	chr4:69363598-69363599	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs537973565	chr4:69363628-69363629	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs146480211	chr4:69363648-69363649	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs557577086	chr4:69363652-69363653	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs35084682	chr4:69363682-69363683	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs35280988	chr4:69363731-69363732	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs553711210	chr4:69363734-69363735	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs573120466	chr4:69363751-69363752	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs563599442	chr4:69363768-69363769	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs138722489	chr4:69363844-69363845	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs575678514	chr4:69363884-69363885	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs149362763	chr4:69363917-69363918	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs563892919	chr4:69363943-69363944	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs147033194	chr4:69364002-69364003	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs138577556	chr4:69364009-69364010	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs540103569	chr4:69364039-69364040	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs560420343	chr4:69364082-69364083	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs181210750	chr4:69364084-69364085	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs186697979	chr4:69364164-69364165	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs189985011	chr4:69364220-69364221	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531429077	chr4:69364234-69364235	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs373061782	chr4:69364257-69364258	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs571014519	chr4:69364258-69364259	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs540052781	chr4:69364319-69364320	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69360800-69364400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr4:69363600-69364000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:69363600-69364000	Enhancers	Fetal Kidney	kidney
4	chr4:69363600-69364200	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr4:69363600-69365000	Enhancers	A549	lung
6	chr4:69363600-69365600	Enhancers	HepG2	liver
7	chr4:69364000-69364400	Enhancers	Fetal Intestine Large	intestine
8	chr4:69364000-69364600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
9	chr4:69364000-69365200	Enhancers	Liver	Liver
10	chr4:69364200-69364600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:69364400-69364600	Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr4:69364400-69364800	Enhancers	Primary hematopoietic stem cells	blood
13	chr4:69364400-69364800	Active TSS	Rectal Mucosa Donor 29	rectum
14	chr4:69364400-69365000	Active TSS	Fetal Intestine Large	intestine
15	chr4:69364400-69365000	Active TSS	Rectal Mucosa Donor 31	rectum
16	chr4:69364600-69364800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr4:69364800-69365000	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr4:69365000-69365400	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr4:69365200-69370400	Weak transcription	Liver	Liver
20	chr4:69369400-69369600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr4:69370200-69370600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:69370400-69370800	ZNF genes & repeats	Liver	Liver
23	chr4:69370600-69371200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr4:69370600-69371200	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr4:69370800-69371200	Enhancers	Primary T cells fromperipheralblood	blood
26	chr4:69370800-69371200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr4:69370800-69371200	Enhancers	Gastric	stomach
28	chr4:69370800-69371200	Enhancers	Spleen	Spleen
29	chr4:69370800-69372000	Weak transcription	Liver	Liver
30	chr4:69371000-69371200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr4:69371200-69372200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr4:69372200-69372400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr4:69373400-69373800	Enhancers	Fetal Heart	heart
34	chr4:69373800-69374200	Weak transcription	Fetal Heart	heart
35	chr4:69374200-69375200	Enhancers	Fetal Heart	heart
36	chr4:69388400-69389000	Enhancers	NHEK	skin
37	chr4:69401800-69402200	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr4:69402000-69402400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr4:69402200-69402600	Strong transcription	Rectal Mucosa Donor 31	rectum
40	chr4:69402400-69411000	Weak transcription	Small Intestine	intestine
41	chr4:69402600-69403200	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr4:69402800-69403400	ZNF genes & repeats	Liver	Liver
43	chr4:69403200-69403800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
44	chr4:69403400-69404800	Strong transcription	Liver	Liver
45	chr4:69403800-69404800	Strong transcription	Rectal Mucosa Donor 31	rectum
46	chr4:69404200-69404600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr4:69404200-69410000	Weak transcription	Colonic Mucosa	Colon
48	chr4:69404600-69406200	Weak transcription	Duodenum Mucosa	Duodenum
49	chr4:69404800-69405600	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr4:69404800-69406800	Weak transcription	Liver	Liver

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